Abstract

ADP-ribosylation factors (ARFs) are approximately 20-kDa guanine nucleotide-binding proteins that serve as GTP-dependent allosteric activators of cholera toxin ADP-ribosyltransferase activity. Four species of mammalian ARF, termed ARF 1-4, have been identified by cloning. Hybridization of a bovine ARF 2 cDNA under low stringency with mammalian poly(A)+ RNA resulted in multiple bands that were subsequently assigned to the known ARF genes using ARF-specific oligonucleotide probes. The relative signal intensities of some bands (e.g. the 3.8- and 1.3-kilobase (kb) mRNAs) that hybridized with the cDNA were not, however, consistent with the intensities observed with the individual ARF-specific oligonucleotide probes. These inconsistencies suggested that other ARF-like mRNAs were comigrating with known ARF mRNAs. To explore this possibility, a cyclic AMP-differentiated HL-60 Lambda ZAP library was screened using the bovine ARF 2 cDNA. Clones corresponding to known ARF genes (1, 3, and 4) were identified by hybridization of positive clones with oligonucleotide probes specific for each ARF species; ARF 2 cDNA-positive, oligonucleotide-negative clones were sequenced. Two new ARF-like genes, ARF 5 and 6, encoding proteins of 180 and 175 amino acids, respectively, were identified. Both proteins contain consensus sequences believed to be involved in guanine nucleotide binding and GTP hydrolysis. ARF 5 was most similar in deduced amino acid sequence to ARF 4, which also has 180 amino acids. ARF 6, whose deduced amino acid sequence is identical with that of a putative chicken pseudogene (CPS1) except for a serine/threonine substitution, was different from other ARF species in size and deduced amino acid sequence. With mammalian poly(A)+ RNA from a variety of tissues and cultured cells, ARF 5 preferentially hybridized with a 1.3-kb mRNA, whereas ARF 6 hybridized with 1.8- and 4.2-kb mRNAs. The fact that the sizes of these mRNAs are similar to those of other ARFs (ARF 1, 1.9 kb; ARF 2, 2.6 kb; ARF 3, approximately 3.8 and 1.3 kb; ARF 4, 1.8 kb) explain the previously observed inconsistencies between the cDNA and ARF-specific oligonucleotide hybridization patterns. All six ARF cDNAs are more similar to each other than to other approximately 20-kDa guanine nucleotide-binding proteins.

Highlights

  • ADP-ribosylation factors (ARFs) a r e -20-kDa gua- Cholera toxin is a secretory product of Vibrio cholerae that nine nucleotide-binding proteins that serve as GTP- is responsible in large part for thedevastatingdiarrheal dependent allosteric activatorsof cholera toxin ADP- syndrome characteristicof cholera [1,2]

  • Clones corresponding to known compounds and proteins unrelated to thceyclase system (11, ARF genes (1,3, and 4) were identified by hybridiza- 12). All of these CT-A-catalyzed reactions are enhanced by tion of positive cloneswith oligonucleotide probes spe- ARF in a GTP-dependent process and are further increased cific for each ARF species; ARF 2 cDNA-positive, oli- by phospholipids and detergents (91, 0, 13, 14)

  • Kinetic analgonucleotide-negativeclones were sequenced.Two yses of these reactions are consistenwt ith the hypothesis that new ARF-like genes, ARF 5 and 6, encoding proteins ARF serves as an allosteric activator of the cholera toxin of 180 and 175 amino acids, respectively, were iden- catalytic unit [13]

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Summary

Retina Spleen Lung Liver

The LTVSALFSRIFGKKQIRILI : Z ~ two clones differed by a single base (position 756 in Fig. 4) in GTTGGCTTGGATGCGGCTGGCAAGACCACAATCCTGTACAAACTGAAGTTGGGGGAGATT : 1 8 0 VGLDAAGKTTILYKLKLGEI: the coding region leading to a different amino acid (Gly in clone 65s; Glu in clone 80) at position 80 in the deduced sequence and at base. Hybridization of Poly(A)+RNA with cDNA and Oligonucleotide. Filters hybridized with the cDNA were washed once with 2. Filters were washed as described for probe GGCACAGAGGGGTCCACTCTCCTGCCTGCTGGGACCTATGGAAGGGGCTTCCTGGCCAAG : E 4 0 ARF 3-1. :lo amino acid sequence comparisons were made using ALIGN [25] and FIG. 3. Nucleotide and deduced amino acid sequences of human ARF 5. The human ARF 5-deduced amino acid sequence is shown in single letter code under the respective codon of the human ARF-5 coding region.

RESULTS
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DISCUSSION
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